Familial temporal lobe epilepsy 7

MONDO:0014639

A temporal lobe epilepsy characterized by autosomal dominant inheritance of focal seizures with prominent auditory symptoms and that has material basis in heterozygous mutation in the RELN gene on chromosome 7q22.

Also known as: ETL7, epilepsy, familial temporal lobe, type 7, familial temporal lobe epilepsy type 7, epilepsy, familial temporal lobe, 7

10 clinical trials for this condition and its sub-types, 0 tagged with Familial temporal lobe epilepsy 7 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Temporal lobe epilepsy (31)

Including sub-types (10) Tagged with Familial temporal lobe epilepsy 7 (0)

Trials to join now! 7 Not yet finished but already full! 2 Completed 1

Routine EEGs may hold hidden clues to childhood epilepsy — a new analysis method is put to the test

Diagnosis Completed

This study is testing whether a computer tool called BioEP can detect signs of seizure susceptibility in standard EEG recordings from children with epilepsy. Researchers will analyze past EEGs from 530 children aged 2 to 18 who already have an epilepsy diagnosis. The goal is to s…

Sponsor: Neuronostics Ltd • Aim: Diagnosis

Last updated Aug 01, 2026 00:00 UTC

Familial temporal lobe epilepsy 7

Where it sits in the disease tree

Routine EEGs may hold hidden clues to childhood epilepsy — a new analysis method is put to the test